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1.
Aesthet Surg J Open Forum ; 4: ojac008, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35592181

RESUMO

Background: Cryolipolysis is an increasingly popular nonsurgical fat-reduction procedure. Published treatment guidance and adverse event (AE) management protocols are limited. Objective: A modified Delphi study aimed to establish global expert consensus on the use of CoolSculpting (Allergan Aesthetics, an AbbVie Company, Irvine, CA), a noninvasive cryolipolysis treatment system. Methods: A literature search informed survey topics for an 11-expert Delphi panel. Panelists completed an online 39-question survey. An interim panel discussion, with open-ended questions and yes/no voting, informed a second survey containing 61 statements, for which panelists rated agreement using a 5-point Likert scale. Topics included treatment outcome and responder definitions, patient evaluation and selection, treatment protocols, patient satisfaction, and AEs. Results: Panelists achieved consensus on 38 final guidelines and recommendations. They reached moderate to complete consensus on 4 statements on defining responders (ie, patients with a range of visible improvement) and 6 statements on patient factors contributing to treatment outcomes (eg, how well the applicator conforms to patient body region). Panelists defined minimum numbers of treatment cycles to achieve visible clinical outcomes for 12 body regions, with moderate to complete consensus on 31 statements. They achieved a strong to complete consensus on 7 statements about patient satisfaction (eg, importance of patient expectations, visible improvement, and before-and-after photographs). Panelists defined management strategies for AEs, with moderate to complete consensus on 15 statements. Conclusions: A modified Delphi process yielded multiple guideline recommendations for cryolipolysis, providing a needed resource for the broad range of clinicians who perform this noninvasive fat-reduction procedure.

2.
J Prim Care Community Health ; 12: 21501327211024431, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34120504

RESUMO

The term "COVID arm" has been coined to describe a harmless delayed hypersensitivity reaction occurring approximately a week after administration of the novel SARS-CoV-2 mRNA vaccine. It appears as a red, warm, pruritic, indurated, or swollen area in the vicinity of the vaccine site. These reactions, especially if accompanied by systemic symptoms, have been mistaken for cellulitis. We report 3 cases of COVID arm, 2 of which were mistaken for cellulitis. Distinguishing features of COVID arm from cellulitis include pruritus as a common finding, occurrence approximately a week after vaccination, a lack of progression of symptoms, rapid response to topical steroids, and/or spontaneous resolution usually over 4 to 5 days.Practice Points:• Patients receiving SARS-CoV-2 vaccines may experience delayed hypersensitivity reactions characterized by erythema, swelling, and itching occurring near the vaccination site (COVID arm), approximately a week after vaccination.• Clinicians can distinguish SARS-CoV-2 vaccine reactions from cellulitis by the time of onset (approximately a week vs 5 days), by the lack of progression of symptoms, and resolution over 4 to 5 days.• Severe cases of COVID arm may be treated with topical steroids.


Assuntos
COVID-19 , Hipersensibilidade Tardia , Vacinas , Braço , Vacinas contra COVID-19 , Celulite (Flegmão)/induzido quimicamente , Celulite (Flegmão)/diagnóstico , Erros de Diagnóstico , Humanos , Hipersensibilidade Tardia/induzido quimicamente , Hipersensibilidade Tardia/diagnóstico , SARS-CoV-2
3.
J Drugs Dermatol ; 20(3): 344-345, 2021 03 01.
Artigo em Inglês | MEDLINE | ID: mdl-33683077

RESUMO

The risk of post-inflammatory hyperpigmentation (PIH) in patients undergoing dermatologic procedures is well known. It is especially common after laser procedures and chemical peels but can be seen with any procedure. PIH is also a sequela of acne, burns, and other trauma. High-risk patients are thought to have excessive production and abnormal distribution of melanin within the skin that triggers PIH, but the exact pathophysiology is unknown.1 We define high-risk patients as Fitzpatrick skin types 3–5, those with existing PIH, or a history of PIH.1,2 Tranexamic acid (TXA) is an antifibrinolytic medication prescribed to treat bleeding and is also used off-label to treat melasma. TXA is contraindicated in patients with hypercoagulable conditions, renal impairment, vision impairment disorders, pregnancy, breast-feeding, or on hormone therapies.3,4,5 From 2015–2020, we have used TXA off-label to successfully treat and/or prevent PIH in approximately 82 high-risk patients after injuries or prior to procedures that disrupt the epidermis. We also have used TXA to prevent PIH after acute injuries such as irritant dermatitis, thermal burns, and abrasions. We now consider TXA treatment for all at risk patients prophylactically before undergoing microneedling, cryotherapy, cryolipolysis, chemical peels, and laser treatments. J Drugs Dermatol. 2021;20(3) doi:344-345. 10.36849/JDD.5622.


Assuntos
Anestésicos Locais/efeitos adversos , Abrasão Química/efeitos adversos , Melanose/tratamento farmacológico , Creme para a Pele/efeitos adversos , Ácido Tranexâmico/administração & dosagem , Acne Vulgar/terapia , Administração Oral , Adulto , Combinação de Medicamentos , Feminino , Humanos , Melanose/etiologia , Uso Off-Label , Resultado do Tratamento , Adulto Jovem
5.
Am J Ophthalmol Case Rep ; 19: 100751, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32490285

RESUMO

PURPOSE: Periorbital myxedema is one the most challenging symptoms for patients with Graves' eye disease (GED). The treatment of this condition is complex and often unsatisfactory. This case demonstrates the use of intralesional hyaluronidase to treat cosmetically concerning periorbital myxedema. OBSERVATIONS: Follow up showed no clinically significant recurrence of myxedema over one year. CONCLUSION: Intralesional hyaluronidase represented an effective and safe treatment of periorbital myxedema in a patient with Graves' eye disease.

6.
Case Rep Dermatol ; 12(1): 1-4, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32009928

RESUMO

Common callouses are formed by the accumulation of keratinocytes in the stratum corneum in response to excess pressure or friction. We report 2 cases of unusual callous formation and an additional 25 more sequential cases that were due to excessive cell phone grip.

7.
J Cosmet Dermatol ; 19(7): 1614-1618, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-31714002

RESUMO

Deoxycholic acid (ATX-101) is a secondary bile acid that was approved as an injectable drug for the reduction of submental fat. Necrosis, an uncommon but serious adverse event, can occur due to inadvertent superficial injection or intra-arterial injection of the acid. The management of the intra-arterial injection of deoxycholic acid has not been well characterized. Here, we discuss methods to decrease the risk of such injections and draw on existing protocols for the inadvertent intra-arterial injection of sclerotherapy solutions and dermal fillers to propose a safe, practical approach to treatment. A case report is presented of a 42-year-old woman who received a deoxycholic acid injection for the correction of submental fullness, which was complicated by the inadvertent intra-arterial injection of the acid. The adaptation of published treatment protocols for the inadvertent injection of sclerosing solutions and dermal fillers allowed for a good outcome in this patient. The inadvertent intra-arterial injection of deoxycholic acid is a rare event. The risk of such injections can be reduced with attention to injection technique and can be managed successfully following the adaptation of protocols in the literature for similar events from vascular compromise due to dermal fillers and sclerosing solutions.


Assuntos
Técnicas Cosméticas , Ácido Desoxicólico , Adulto , Técnicas Cosméticas/efeitos adversos , Ácido Desoxicólico/efeitos adversos , Feminino , Humanos , Injeções , Injeções Intra-Arteriais , Injeções Subcutâneas , Escleroterapia
9.
Appl Neuropsychol Child ; 5(1): 50-5, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-25650638

RESUMO

Development of emotion regulation strategy use involves a transition from reliance on suppression during childhood to greater use of reappraisal in adolescence and adulthood-a transition that parallels developmental changes in executive functions. We evaluated the relationship between emotion regulation strategy use and executive functioning in the everyday life of 70 typically developing adolescents who completed the Emotion Regulation Questionnaire for Youth and the Behavior Rating Inventory of Executive Function-Self-Report. Results indicated that greater reliance on reappraisal was associated with better executive functions, while reliance on suppression was related to poorer executive functions. Findings suggest that adolescents who rely on reappraisal may have more cognitive resources to help them remain attentive and well regulated in their daily lives. On the other hand, if better executive functions facilitate the use of reappraisal, adolescents' ability to regulate their emotions could potentially be enhanced via supports for executive functions.


Assuntos
Desenvolvimento do Adolescente/fisiologia , Emoções/fisiologia , Função Executiva/fisiologia , Autocontrole , Adolescente , Feminino , Humanos , Masculino
10.
Alzheimer Dis Assoc Disord ; 8(Suppl. 4): 38-48, 1994.
Artigo em Inglês | MEDLINE | ID: mdl-11657672

RESUMO

Despite the need for minority subjects in research studies of Alzheimer disease (AD), the successful involvement of minority patients in such studies has been difficult. This report discusses the many societal, economic, logistical, and attitudinal barriers that have inhibited the participation of minority patients and their families in medical research programs of AD. Special consideration is given to the unique cultural issues that arise when conducting studies involving African-American elderly subjects. Methods are considered for overcoming the barriers to participation gleaned from the national study CERAD (Consortium to Establish a Registry of Alzheimer Disease) and other investigations of AD. Recommendations are made for future research programs targeted on the specific health care needs and concerns of the minority segments of our population.


Assuntos
Idoso , Doença de Alzheimer/etnologia , Negro ou Afro-Americano , Ensaios Clínicos como Assunto/legislação & jurisprudência , Demência , Experimentação Humana , Grupos Minoritários/legislação & jurisprudência , Fatores Socioeconômicos , Negro ou Afro-Americano/legislação & jurisprudência , Negro ou Afro-Americano/psicologia , Doença de Alzheimer/diagnóstico , Doença de Alzheimer/psicologia , Atitude , Comunicação , Diversidade Cultural , Economia , Educação , Pesquisa Empírica , Família , Educação em Saúde , Acessibilidade aos Serviços de Saúde/legislação & jurisprudência , Hispânico ou Latino , Serviços de Assistência Domiciliar , Humanos , Disseminação de Informação , Serviços de Informação , Jurisprudência , Métodos , Motivação , Seleção de Pacientes , Pesquisa , Projetos de Pesquisa , Sujeitos da Pesquisa , Má Conduta Científica , Valores Sociais , Seguridade Social , Experimentação Humana Terapêutica , Confiança , Estados Unidos
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